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Comparison of sacubitril valsartan with amilodipine valsartan in chronic renal failure patients

Comparison effect of sacubitril valsartan with amilodipine valsartan on echocrardiographic findings and kidney function indicators in chronic renal failure patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250805066770N1
Enrollment
90
Registered
2025-09-10
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic kidney disease. Chronic kidney disease (CKD)

Interventions

Intervention 1: Intervention group : Investigating the effect of sacubitril valsartan on echocardiographic characteristics and renal function indices in patients with chronic renal failure. Interventi

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with chronic renal failure over 18 years of age (uACR = 30 mg/g, GFR < 60 ml/min/1.73m2) 2. Patients with no contraindications or known tolerance to ARB 3. Patients without bilateral renal artery stenosis 4. Patients without nephrotic syndrome (350 mg/g) < urine protein: creatinine ratio or 300 mg/mmol < uACR or (Alb < 35 g/l) 5. Patients not taking immunosuppressive drugs 6. Patients not taking heparin or enoxaparin 7. Women other than pregnant, lactating women and all women who plan to become pregnant in the next 6 months 8. In case of alcohol consumption, a maximum of 2 ounces per day for men and 1 ounce per day for women and people without drug use 9. People without active malignancy 10. Patients who are able to stop their previous antihypertensive drugs

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Age, gender, systolic blood pressure, albuminuria, history of diabetes, plasma and urinary electrolytes, lipid profile, plasma albumin hs, CRP, Ejection Fraction, BMI, GFR, smoking status, diastolic blood pressure, pulmonary artery pressure, mitral regurgitation. Timepoint: At the beginning of the study, the first month, the third month, and the sixth month. Method of measurement: Laboratory sampling.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Amoutaghi

Kashan University of Medical Sciences

Z.amoutaghi@gmail.com+98 31 5544 3022

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026